Canonical Allele Identifier: CA2679876751
Gene: SOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634735_107634736del , CM000668.2:g.107634735_107634736del GRCh38
NC_000006.11:g.107955939_107955940del , CM000668.1:g.107955939_107955940del GRCh37
NC_000006.10:g.108062632_108062633del NCBI36
NG_028200.1:g.149623_149624del
NG_028200.2:g.149623_149624del

Transcript Alleles

HGVS Amino-acid change
ENST00000317357.10:c.1891_1892del MANE Select ENSP00000318900.5:p.Pro631GlyfsTer?
ENST00000317357.9:c.1891_1892del ENSP00000318900.5:p.Pro631GlyfsTer?
NM_018013.3:c.1891_1892del NP_060483.3:p.Pro631GlyfsTer?
XM_005267041.3:c.2044_2045del XP_005267098.1:p.Pro682GlyfsTer?
XM_005267042.3:c.1948_1949del XP_005267099.1:p.Pro650GlyfsTer?
XM_011535920.1:c.2044_2045del XP_011534222.1:p.Pro682GlyfsTer?
XM_011535921.1:c.1930_1931del XP_011534223.1:p.Pro644GlyfsTer?
XM_011535922.1:c.1303_1304del XP_011534224.1:p.Pro435GlyfsTer?
XM_011535923.1:c.1114_1115del XP_011534225.1:p.Pro372GlyfsTer?
XM_005267041.4:c.2044_2045del XP_005267098.1:p.Pro682GlyfsTer?
XM_005267042.4:c.1948_1949del XP_005267099.1:p.Pro650GlyfsTer?
XM_011535920.2:c.2044_2045del XP_011534222.1:p.Pro682GlyfsTer?
XM_011535921.2:c.1930_1931del XP_011534223.1:p.Pro644GlyfsTer?
XM_011535923.2:c.1114_1115del XP_011534225.1:p.Pro372GlyfsTer?
XM_017010991.1:c.1444_1445del XP_016866480.1:p.Pro482GlyfsTer?
XM_017010992.1:c.1444_1445del XP_016866481.1:p.Pro482GlyfsTer?
XM_017010993.1:c.1444_1445del XP_016866482.1:p.Pro482GlyfsTer?
XM_017010994.1:c.1444_1445del XP_016866483.1:p.Pro482GlyfsTer?
NM_018013.4:c.1891_1892del MANE Select NP_060483.3:p.Pro631GlyfsTer?